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An association of tubular dysfunction, cortical macrocysts and chronic kidney disease

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Abstract

We present an unusual combination of kidney disorders in a boy born to consanguineous parents. He presented in the first year of life with dehydration and urosepsis and was subsequently found to have hyposthenuria and distal renal tubular acidosis, with normal appearance of the kidneys, by ultrasound examination. By 4 years of age he had developed multiple large cysts in both kidneys, and his nephropathy eventually progressed so that at 17 years of age he is approaching end-stage renal disease (ESRD). The association of initial tubular dysfunction followed by the development of multiple cysts may represent a new form of kidney disease.

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References

  1. Torres VE, Young WF Jr, Offord KP, Hattery RR (1990) Association of hypokalemia, aldosteronism, and renal cysts. N Engl J Med 322:345–351

    Article  PubMed  CAS  Google Scholar 

  2. Gurgey A, Ozalp I, Rotig A, Coskun T, Tekinalp G, Erdem G, Akeoren Z, Caglar M, Bakkaloglu A (1996) A case of Pearson syndrome associated with multiple renal cysts. Pediatr Nephrol 10:637–638

    Article  PubMed  CAS  Google Scholar 

  3. Buemi M, Allegra A, Rotig A, Gubler MC, Aloisi C, Corica F, Pettinato G, Frisina N, Niaudet P (1997) Renal failure from mitochondrial cytopathies. Nephron 76:249–253

    Article  PubMed  CAS  Google Scholar 

  4. Hildebrandt F, Omram H (2001) New insights: nephronophthisis–medullary cystic kidney disease. Pediatr Nephrol 16:168–176

    Article  PubMed  CAS  Google Scholar 

  5. Hoefele J, Otto E, Felten H, Kuhn K, Bley TA, Zauner I, Hildebrandt F, Neumann HP (2004) Clinical and histological presentation of 3 siblings with mutations in the NPHP4 gene. Am J Kidney Dis 43:358–364

    Article  PubMed  CAS  Google Scholar 

  6. Bingham C, Hattersley AT (2004) Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1beta. Nephrol Dial Transplant 19:2703–2708

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Detlef Bockenhauer.

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Bockenhauer, D., Rees, L. & van’t Hoff, W. An association of tubular dysfunction, cortical macrocysts and chronic kidney disease. Pediatr Nephrol 21, 580–583 (2006). https://doi.org/10.1007/s00467-006-0009-6

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  • DOI: https://doi.org/10.1007/s00467-006-0009-6

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